510(k) K920536 ยท LIO Device, Specimen Collection
AFFIRM VP SAMPLE COLLECTION SET
| Applicant | Microprobe Corp., Bothell WA, US |
| Decision | Substantially Equivalent, Jul 30, 1992 |
| Received | Feb 5, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920536
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.